FDA.reportPublic FDA data

Exoflow™

Primary DI
10859273007172
Brand
Exoflow™
Company
RELIGN CORPORATION
Model
R-10017
Catalog number
R-10017
Device description
Fluid management accessory disposable, outflow only
Published
2020-02-20
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K162770000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K162770000Relign SystemRelign Corporation2017-01-04GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10859273007172PackageGS16In Commercial Distribution
08592730070177PreviousGS10
00859273007175PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085927300717210859273007172
08592730070177085927300701778592730070177
00859273007175008592730071758592730071750859273007175

GMDN Terms#

Term, Definition table
TermDefinition
Surgical irrigation/aspiration tubing setA collection of flexible, noninvasive, double-lumen tubing and associated items intended to provide twin conduits in a surgical irrigation/aspiration system to deliver irrigation solution (e.g., saline) from its source (e.g., gravity feed bag) to a surgical cannula (not included) through one lumen, and provide aspiration (suction) through the other lumen (i.e., enables both irrigation and aspiration), during a surgical procedure (e.g., dental, laparoscopy). The tubing set includes devices such as clamps, filters, spikes, and Y-piece connectors, and may in addition include an integrated manual pump (e.g., a squeeze bulb) or handpiece. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
(866) 608-0131customer.service@religncorp.com

Regulatory Flags#

DUNS number
080031617
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024681101STANDARD SHAVER™ 4.2MMR10029R100292025-10-07
008890246811184.2MM CURVED STANDARD SHAVER™R10030R100302025-10-07
00859273007052Dynablator™R-10005R-100052020-02-20
008592730070833-in-1 SHAVER™ 4.2mmR-10008R-100082020-07-17
00859273007120Standard Shaver 3.4mmR-10012R-100122021-03-05
008592730071443-in-1 SHAVER™ 5.0mmR-10014R-100142020-02-20
00859273007175Exoflow™R-10017R-100172020-02-20
00859273007243Curved Standard Shaver 3.4mmR-10024R-100242021-03-05
00859273007250Curved Standard Ball Burr XL 5.0 mmR-10025R-100252022-06-16
00859273007267Curved Standard Shaver XL 4.2 mmR-10026R-100262022-06-16
00859273007274Curved Dynablator® XLR-10027R-100272024-12-18
00859273007212Standard Burr 5.0mmR-10021R-100212020-10-14
00859273007236Tricera™ Handpiece, AutoclavableR-10023R-100232020-08-20
00859273007014Tricera™ ControllerR-10001R-100012020-02-20
00859273007021Tricera™ HandpieceR-10002R-100022020-02-20
00859273007038Veriflow™R-10003R-100032020-02-20
00859273007113Tricera™ Handpiece, AutoclavableR-10011R-100112020-02-20
10859273007271Curved Dynablator® XLR-10027R-100272024-12-18
10859273007257Curved Standard Ball Burr XL 5.0 mmR-10025R-100252022-06-16
10859273007264Curved Standard Shaver XL 4.2 mmR-10026R-100262022-06-16

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00197998302718Solventum™Solventum US LLCGEI2026-09-25
00724995269586Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
00724995269951Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
00724995269968Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
00190776432300MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432317MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432324MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432430MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432447MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432454MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776431457MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776432041MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776432195MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776432201MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776431181MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431198MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431204MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431211MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431228MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431235MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431242MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431259MillenniumAvalign Technologies, Inc.GEI2026-09-21
10840113236852BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113236890BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113236937BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237040BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237064BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237101BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237118BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237132BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21